{"id":13076,"date":"2024-08-23T05:37:00","date_gmt":"2024-08-23T03:37:00","guid":{"rendered":"https:\/\/valintermed.com\/?p=13076"},"modified":"2024-08-23T05:37:00","modified_gmt":"2024-08-23T03:37:00","slug":"spinotserebellyarnaya-degeneratsiya-i-distrofiya-rogovitsy","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/spinal-cord-degeneration-and-rogovitsy-dystrophy\/","title":{"rendered":"Spinocerebellar degeneration and corneal dystrophy"},"content":{"rendered":"
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Spinocerebellar degeneration (SCD) is a group of inherited neurodegenerative diseases that lead to progressive destruction of neurons in the spinal cord and cerebellum. The main manifestations of this disease are ataxia, dysplasia, impaired coordination of movements and progressive muscle weakness, which significantly worsens the quality of life of patients. The disease can have various forms, differing in genetic mechanisms, clinical manifestations and rates of progression. In some cases, clinical symptoms of spinocerebellar degeneration are accompanied by manifestations from other systems, including changes in the function of the eyes, hearing and psychoemotional disorders, which complicates diagnosis and treatment.<\/p>\n

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